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Director Statistical Programming Jobs in Pittsburgh, PA

... Engineering, Finance, Government/Public Policy, Health Administration/Public Health ... Mathematics/Statistics, Operations/Supply Chain, Organizational Management/Behavior, Risk ...

You will leverage skills in data manipulation, visualisation, and statistical modelling to support ... Data Engineer / Azure Solutions Architect - Google Professional Data Engineer - DAMA CDMP ...

Selects appropriate principles of engineering economics, and probability and statistics to analyze ... Mentor direct reports and other engineers. * Demonstrates professional attitudes relevant to the ...

Direct-Hire/Permanent Hours: Standard business hours Start: May Overview: Join a cutting-edge lab ... Strong expertise in statistical analysis and data interpretation * Proficiency in programming ...

Direct-Hire/Permanent Hours: Standard business hours Start: May Overview: Join a cutting-edge lab ... Strong expertise in statistical analysis and data interpretation * Proficiency in programming ...

Direct-Hire/Permanent Hours: Standard business hours Start: May Overview: Join a cutting-edge lab ... Strong expertise in statistical analysis and data interpretation * Proficiency in programming ...

Manager, Engineering

Pittsburgh, PA · On-site +1

$115K - $214K/yr

Direct and/or participate in client meetings/job site visits to collect or deliver design and ... Ability to independently work with mathematical concepts such as probability and statistical ...

Direct and/or participate in client meetings/job site visits to collect or deliver design and ... Ability to independently work with mathematical concepts such as probability and statistical ...

Selects appropriate principles of engineering economics, and probability and statistics to analyze ... Mentor direct reports and other engineers. * Demonstrates professional attitudes relevant to the ...

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Director Statistical Programming information

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How much do director statistical programming jobs pay per year?

As of Aug 23, 2026, the average yearly pay for director statistical programming in Pittsburgh, PA is $271,972.00, according to ZipRecruiter salary data. Most workers in this role earn between $252,900.00 and $313,100.00 per year, depending on experience, location, and employer.

What is a director statistical programming?

The job of a director of statistical programming oversees the development and implementation of SAS programs to produce statistical analysis datasets. In this career, your responsibilities include managing the team that generates tables and graphs using the SAS programs for applications such as clinical studies. Other duties include participating in the planning and review of statistical analysis and studying reports, abstracts, and manuscripts as required. You collaborate with project leads to contribute to department operations and standards, such as CDISC for clinical research.

What does a director statistical programming do?

A Director of Statistical Programming oversees teams responsible for the programming and analysis of clinical trial data, ensuring the accuracy and integrity of statistical outputs. They set departmental strategies, manage resources, and ensure compliance with regulatory requirements and industry standards. This role also involves collaborating with other departments, such as biostatistics and clinical operations, to support the successful delivery of statistical analyses for drug development and regulatory submissions. They play a key leadership role in mentoring staff and advancing programming processes and technologies.

What are the key skills and qualifications needed to thrive as a director statistical programming?

To thrive as a Director of Statistical Programming, you need advanced expertise in statistical analysis, programming languages such as SAS or R, and a strong background in clinical trial data, typically supported by a degree in statistics, mathematics, or a related field. Familiarity with regulatory submission processes, CDISC standards, and project management tools is essential, as are relevant certifications like SAS Certified Professional. Leadership, effective communication, and strategic thinking are key soft skills for managing teams and collaborating across departments. These skills ensure high-quality data outputs, regulatory compliance, and successful execution of complex clinical development projects.

How does a director statistical programming typically collaborate with cross-functional teams in a pharmaceutical or biotech company?

A Director of Statistical Programming regularly works with biostatistics, clinical data management, regulatory affairs, and medical writing teams to ensure that statistical deliverables meet project timelines and regulatory requirements. They coordinate programming efforts across multiple studies, provide leadership and mentorship to programming staff, and help resolve technical or resource-related challenges. Effective collaboration is essential to streamline workflows, maintain data integrity, and ensure clear communication of statistical results within the organization.

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Engineer Sr,Supplier Quality

Eos Energy Enterprises

Warrendale, PA • On-site

Full-time

Posted 18 days ago


Job description

About Eos Energy Enterprises
Eos Energy Enterprises, Inc. is accelerating the shift to American energy independence with positively ingenious solutions that transform how the world stores power. Our breakthrough Znyth™ aqueous zinc battery was designed to overcome the limitations of conventional lithium-ion technology. It is safe, scalable, efficient, sustainable, manufactured in the U.S., and the core of our innovative systems that today provides utility, industrial, and commercial customers with a proven, reliable energy storage alternative for 3 to 12-hour applications. Eos was founded in 2008 and is headquartered in Edison, New Jersey. For more information about Eos (NASDAQ: EOSE), visit eose.com.
Overall Job Summary:
The Senior Supplier Quality Engineer owns and drives the technical rigor and effectiveness of the supplier quality program for our battery energy storage systems (BESS) - spanning all aspects of the BESS, such as the modules, packs, battery management systems (BMS), thermal management, enclosures, and power conversion components. This role is the technical authority linking engineering, manufacturing, and the global supply base, ensuring supplier materials and processes meet safety, performance, and reliability requirements for grid-scale and behind-the-meter energy storage. The engineer drives root cause resolution, qualification rigor, and continuous improvement across a supply chain where safety and long-term degradation performance are mission critical.
Job Responsibilities:
  • Own the technical strategy and rigor of the supplier quality program both for the BESS and BOS (balance-of-system) suppliers, setting inspection criteria, sampling plans, and acceptance methods
  • Lead supplier qualification and PPAP/APQP (or equivalent) for new parts, designs, and manufacturing process changes, including first-article and pilot-run approval
  • Drive root cause analysis (8D, 5-Why, fishbone) for supplier-related nonconformances and verify corrective action effectiveness
  • Conduct and lead supplier audits and process capability assessments at manufacturing sites; develop supplier scorecards and drive improvement plans
  • Partner with engineering to define incoming inspection requirements, critical-to-quality (CTQ) characteristics, and acceptance criteria for all supplied parts or services
  • Review and approve supplier PPAPs, control plans, FMEAs, and battery test reports (cycle life, abuse/safety, thermal runaway propagation, environmental)
  • Ensure supplier compliance with battery safety and transport standards, including UL 1973, UL 9540/9540A, IEC 62619, IEC 63056, UN 38.3, and applicable UL 1642/IEC 62133 cell-level requirements
  • Lead containment and disposition decisions for nonconforming supplier material (MRB), including cell/pack quarantine and safe-handling protocols
  • Establish statistical process control (SPC) requirements and monitor supplier process and cell performance trends (capacity, impedance, IR, yield) over time
  • Support supplier corrective action tied to field returns, warranty claims, and degradation/safety incident investigations
  • Mentor quality engineers and build technical capability within the SQE team
  • Present quality metrics, risk assessments, and improvement roadmaps to leadership and key customers

Education/Experience:
  • Bachelor's degree in Electrical, Mechanical, Chemical, Materials, or Industrial Engineering, or related technical field (advanced degree a plus)
  • 6+ years of experience in supplier quality, quality engineering, or manufacturing quality, with direct supplier-facing responsibility; experience with lithium-ion cells, battery packs, or energy storage systems strongly preferred
  • Demonstrated expertise in APQP/PPAP, FMEA, SPC, MSA, and root cause/corrective action methodologies
  • Working knowledge of battery cell chemistry, construction (cylindrical, prismatic, pouch), and failure modes (thermal runaway, capacity fade, internal short circuit)
  • Familiarity with battery safety and performance standards: UL 1973, UL 9540A, IEC 62619, IEC 62620, UN 38.3, UN/DOT transport requirements, and relevant grid-interconnection or NFPA 855 considerations
  • Experience auditing suppliers against ISO 9001, IATF 16949, or ISO 9001-based battery manufacturing quality systems
  • Strong working knowledge of GD&T, mechanical/electrical drawing interpretation, and dimensional and electrical inspection methods (capacity, impedance, OCV, insulation resistance)
  • Familiarity with statistical tools and quality software (Minitab, QMS platforms, SPC systems) and battery test data analysis
  • Excellent cross-functional communication skills; able to influence suppliers and internal stakeholders without direct authority
  • ASQ certification (CQE, CSQP) or Six Sigma Black/Green Belt preferred

Skills/Abilities:
  • Advanced knowledge of supplier quality management systems, quality planning, and manufacturing process controls.
  • Expert understanding of APQP, PPAP, Control Plans, PFMEA/DFMEA, MSA, SPC, and corrective action methodologies.
  • Strong knowledge of lithium-ion battery technologies, battery management systems (BMS), energy storage systems (ESS/BESS), and associated manufacturing processes.
  • Ability to evaluate supplier manufacturing capabilities, process controls, and quality systems to ensure compliance with product and customer requirements.
  • Proficiency in interpreting mechanical drawings, electrical schematics, specifications, GD&T, and inspection requirements.
  • Experience with dimensional, electrical, and functional inspection methods and validation testing.
  • Strong understanding of reliability, safety, risk assessment, and failure analysis methodologies

Travel
  • Local Travel: 25 - 40% domestic travel to supplier and cell/pack manufacturing sites

Working Conditions
  • Office Environment - Must be able to remain in a stationary position 50% of the time and occasionally move about inside the office to access file cabinets, office machinery, etc. Required to have close visual acuity to perform an activity such as: preparing and analyzing data and figures; transcribing; viewing a computer terminal; extensive reading. May be required to exert up to 25 pounds of force occasionally to lift, carry, push, pull or otherwise move objects, including the human body.
  • Factory - The worker may be subject to hazards. Includes a variety of physical conditions, such as proximity to moving mechanical parts, vibration, moving vehicles, electrical current, exposure to temperature changes or exposure to chemicals. While performing the duties of this job, the employee may be exposed to fumes, airborne particles, odors, dust, mists, and gases. The noise level in the work environment can be loud. Required to have close visual acuity to perform an activity such as: preparing and analyzing data and figures; transcribing; viewing a computer terminal; extensive reading; visual inspection involving small defects, small parts, and/or operation of machines (including inspection); using measurement devices; and/or assembly or fabrication parts at distances close to the eyes. Machinery operation requires the use of safety equipment to include but not limited to eye safety glasses, hearing protectors, work boots, and lab coats. May be required to exert up to 50 pounds of force occasionally to lift, carry, push, pull or otherwise move objects, including the human body.